Micropulse diode treatment in refractory neovascular glaucoma, high-energy level combined with adjunctive Ranibizumab

Hazem Helmy
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Abstract

Introduction: Neovascular glaucoma is one of the highly refractory glaucoma types that mandates frequent modification of treatment. Micropulse diode cyclophotocoagulation may be a good option, but it may need an adjunctive and modification of parameters away from standard protocol. Design: A prospective, cohort, interventional case study. Purpose: To assess the safety and efficacy of high energy level of micropulse (MP) diode laser application after intravitreal injection of ranibizumab in the treatment of neovascular glaucoma refractory to medical treatment. Patients and Methods: This is a prospective, interventional, cohort, randomized case series study that included patients with neovascular glaucoma refractory to medical treatment. All patients underwent intravitreal injection of ranibizumab and then MP diode transscleral cyclophotocoagulation treatment in a high energy level. All patients were followed up for 24 months. The primary outcome measure was IOP reduction; the secondary outcome measure was stability and number of retreatment sessions; and the third outcome measure was complications. Results: This study included 50 eyes of 50 patients, 52% of them were male while 48% were female. Age of the studied patients ranged between 42 and 74 years with a mean of 60.8 ± 7.6 years. Cause of neovascular glaucoma was diabetes in 31 (62%), RVO in 8 (16%), and ocular ischemic syndrome in 3 (6%) of cases. The mean preoperative IOP was 41.2 ± 5.8 mmHg that decreased to 17.62 ± 2.01, 19 ± 4.05, 18.16 ± 1.96, 18.38 ± 1.96, 18.12 ± 1.98, and 18.3 ± 2.18 mmHg at 1, 3, 6, 12, 18, and 24 months, respectively (P < 0.001). Antiglaucoma treatment significantly decreased from 3.00 to 2.00 (P < 0.001). Success was achieved in 44 (88%) cases, whereas failure was met in 6 (12%) cases. Qualified success was met in 43 (97.2%) succeeded cases, whereas 1 (2.8%) succeeded case was signed under complete success. No major complications were encountered and none of the patients lost vision. Conclusion: Micropulse diode cyclophotocoagulation in high energy level can be a safe and effective noninvasive line of treatment in patients with neovascular glaucoma that may last for up to 24 months. Adjunctive use of intravitreal ranibizumab may improve results and decrease complications.
微脉冲二极管治疗难治性新生血管性青光眼,高能水平联合辅助雷尼单抗
简介:新生血管性青光眼是高度难治性青光眼类型之一,需要经常修改治疗方案。微脉冲二极管光凝可能是一个很好的选择,但它可能需要辅助和参数修改远离标准方案。设计:前瞻性、队列、干预性案例研究。目的:评价雷尼单抗玻璃体内注射后应用高能微脉冲(MP)二极管激光治疗难治性新生血管性青光眼的安全性和有效性。患者和方法:这是一项前瞻性、介入性、队列、随机病例系列研究,纳入了难治性新生血管性青光眼患者。所有患者均接受雷尼珠单抗玻璃体内注射,然后进行高能MP二极管经巩膜环光凝治疗。所有患者随访24个月。主要结局指标为IOP降低;次要结局指标是稳定性和再治疗次数;第三个结果是并发症。结果:本研究纳入50例患者50只眼,男性占52%,女性占48%。患者年龄42 ~ 74岁,平均60.8±7.6岁。新血管性青光眼的病因为糖尿病31例(62%),RVO 8例(16%),眼缺血综合征3例(6%)。术前平均IOP为41.2±5.8 mmHg, 1、3、6、12、18、24个月时分别降至17.62±2.01、19±4.05、18.16±1.96、18.38±1.96、18.12±1.98、18.3±2.18 mmHg (P < 0.001)。抗青光眼治疗从3.00显著降低到2.00 (P < 0.001)。成功44例(88%),失败6例(12%)。成功43例(97.2%),完全成功1例(2.8%)。没有发生严重并发症,也没有患者失明。结论:高能微脉冲二极管光凝治疗新血管性青光眼是一种安全有效的无创治疗方法,治疗期可达24个月。辅助使用玻璃体内雷尼珠单抗可以改善结果并减少并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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